Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Carbonochloridic acid, octyl ester | HCID 81956 | — |
| Edukt | HCID 178507852 | HCID 178507852 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 178443805 | HCID 178443805 | — |
Reaktionsschritte
10 G. of 2,4-diamino-6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxide are suspended in 150 ml. of methylene chloride and 20 ml. of triethylamine. The suspension is cooled to 5° C. and 28 g. of chloroformic acid octyl ester are added dropwise while stirring. The mixture is cooled for 30 minutes and then stirred at room temperature for 1 hour. The mixture is extracted with methylene chloride, washed with water, dried over magnesium sulfate and evaporated under reduced pressure. The residue is recrystallized from methylene chloride/ethanol, there being obtained dioctyl 6-[3,6-dihydro-1(2H)-pyridyl]-2,4-pyrimidine-dicarbamate-3-oxide, having a melting point of 64° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04175189 |
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| Quelldatensatz | uspto-grants-1979_11 |
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| ORD ID | ord-0d5dd75d51ec4fc482b08a21147b6ca6 |
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| Quellennotiz | uspto-grants-1979_11 |
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